Frau Camille, Boursicot Pierre-Yves
Groupement D'Intérêt Paléontologique, Science et Exposition, 35 Impasse lieutenant Daumas, 83100, Toulon, France.
, 14, rue Joannes, R49450, Villedieu-la-Blouère, France.
BMC Ecol Evol. 2021 Jun 26;21(1):133. doi: 10.1186/s12862-021-01857-y.
Expression of sexual dimorphism is recognised in various fossil groups of molluscs such as the Ammonoidea, an extinct group of shelled cephalopods. During the Mesozoic, the best-documented sexual dimorphic examples are seen in the Jurassic superfamily Perisphinctoidea. It is usually expressed by distinct adult size and apertural modifications between the antidimorphs. Putative males (otherwise referred to as microconch) are small in size and develop lappets at the end of the shell while the females (macroconch) are larger and bear a simple peristome. Dubious cases are, however, known in that superfamily, which often relate to taxonomic biases or lack of diagnostic characters, and some others expose ontogenetic anomalies illustrated by 'sex reversals' in the shell morphology and ornamentation.
The discovery of two specimens of the Callovian Aspidoceratidae Peltoceras athleta (Phillips), having both female and male features, questions the significance and causes of 'sex reversals' in the Ammonoidea. The two specimens have started with the macroconch ontogeny of Peltoceras athleta and show an apparent change toward maleness in the adult, as illustrated by their rounded whorl section, ribs retroversion, fading of the tubercles and lappets typical of the microconchs. Few other cases of female-to-male, as well as male-to-female 'sex reversal', are known in the fossil record, all belonging to the Jurassic Perisphinctoidea (families Perisphinctidae or Aspidoceratidae). Since all Jurassic Perisphinctoidea are strictly gonochoristic, these 'sex reversals' are pathological in nature and are herein referred to as a new forma-type pathology: namely "forma hermaphrodita".
In the absence of any clear evidence of injury or parasitism, we hypothesize that such "forma hermaphrodita" individuals illustrate pathologic cases of intersexuality. Little is known about the ammonoid soft parts, and it is not possible to determine which internal sexual organs occur in specimens having both male and female external shell features. Abnormal feminisation and/or masculinisation also occur in modern cephalopods, the latter also grouping only gonochoric species. This phenomenon is similarly illustrated by a change in the adult body size and a mixing of both female and male structures. In that case, intersexuality is either advantageous in the population or caused sterility. The causes of intersexuality are not clearly established but environmental pollutants are evoked in modern cephalopods because they act as endocrine disrupters. 'Sex reversals' and/or non-functional reproductive abnormalities have also been caused by endocrine disrupters in various gonochoric gastropods species, but infestation, genetic abnormalities, temperature fluctuations or viruses are multiple causes, which can stimulate or inhibit neural-endocrinal activity by direct gonadal influence, and ultimately lead to feminisation or masculinisation in fishes, isopods, crustaceans, and gastropods as well. Regardless of whether "forma hermaphrodita" is due to an exogenic or endogenic cause, the record of intersex Perisphinctoidea in the Jurassic can be explained by the ready recognition of dimorphic pairs, and the easy collection of large and sufficiently preserved fossil palaeopopulations in which intersex specimens have statistically more chance to be found.
性二态性在软体动物的各种化石类群中都有体现,比如菊石亚纲,这是一类已灭绝的有壳头足类动物。在中生代,记录最详尽的性二态性例子见于侏罗纪的超科——旋环菊石超科。它通常表现为成年个体大小不同以及反形态之间的口部形态差异。假定的雄性(也称为微壳型)体型较小,在壳的末端发育出叶状突,而雌性(巨壳型)体型较大,口缘简单。然而,在那个超科中存在一些可疑情况,这些情况往往与分类学偏差或缺乏诊断特征有关,还有一些则表现为壳形态和纹饰中出现“性反转”所显示的个体发育异常。
卡洛维阶的箭石科强壮佩尔托菊石(菲利普斯)的两个标本被发现,它们兼具雌性和雄性特征,这对菊石亚纲中“性反转”的意义和原因提出了质疑。这两个标本最初具有强壮佩尔托菊石的巨壳型个体发育特征,在成年时显示出向雄性特征的明显转变,表现为其螺环截面圆润、肋向后弯曲、微壳型典型的瘤和叶状突消失。在化石记录中,已知很少有其他从雌性到雄性以及从雄性到雌性的“性反转”案例,它们都属于侏罗纪的旋环菊石超科(旋环菊石科或箭石科)。由于所有侏罗纪的旋环菊石超科都是严格的雌雄异体,这些“性反转”本质上是病理性的,在此被称为一种新的形态类型病理学:即“雌雄同体形态”。
在没有任何明显的损伤或寄生证据的情况下,我们推测这种“雌雄同体形态”个体代表了雌雄间性的病理案例。关于菊石的软体部分所知甚少,无法确定具有雌雄两性外壳特征的标本中存在哪些内部性器官。现代头足类动物中也会出现异常的雌性化和/或雄性化现象,后者同样只包括雌雄异体的物种。这种现象同样表现为成年个体大小的变化以及雌性和雄性结构的混合。在这种情况下,雌雄间性在种群中要么具有优势,要么导致不育。雌雄间性的原因尚未明确,但现代头足类动物中提到环境污染物,因为它们可作为内分泌干扰物。内分泌干扰物也在各种雌雄异体的腹足类物种中导致了“性反转”和/或无功能的生殖异常,但感染、基因异常、温度波动或病毒也是多种原因,它们可通过直接影响性腺来刺激或抑制神经内分泌活动,最终导致鱼类、等足类、甲壳类和腹足类动物出现雌性化或雄性化。无论“雌雄同体形态”是由外源性还是内源性原因引起的,侏罗纪旋环菊石雌雄间性的记录都可以通过对二态性配对的易于识别以及对大型且保存充分的化石古种群的轻松采集来解释,在这些古种群中,雌雄间性标本在统计学上更有可能被发现。